Affiliation:
1. Department of Biochemistry and Biophysics, University of Rochester Medical Center, Rochester, New York
Abstract
Biliverdin reductase (BVR) functions in cell signaling through three distinct tracks: a dual-specificity kinase that functions in the insulin receptor/MAPK pathways ( 25 , 29 , 51 ); a bzip-type transcription factor for ATF-2/CREB and HO-1 regulation ( 1 , 25 ); and a reductase that catalyzes the conversion of biliverdin to bilirubin ( 27 ). These, together with the protein’s primary and secondary features, intimately link BVR to the entire spectrum of cell-signaling cascades.
Publisher
American Physiological Society
Cited by
116 articles.
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